Syner-KINASE 10,000IU powder for solution for injection or infusion (CLDA (15)A/14)
Yes – this has been recalled
- The problem
- Specific batch manufactured by Syner-Medica Ltd is being recalled due to concerns it may go out of specification for potency before it expires.
- What to do
- Check the batch number on your pack against the list below. Do not stop taking a prescribed medicine without talking to your pharmacist, GP or prescriber first – they can check your supply and swap it if needed.
Source: Medicines and Healthcare products Regulatory Agency (MHRA)
Official notice ↗
Product information
CLDA number
CLDA (15)A/14
MDR number
MDR 43-12/15
Company name
Syner-Medica Limited
Product description
Syner-KINASE 10,000IU powder for solution for injection or infusion
PL: 20675/0006
Batch number/expiry
| Batch no | Expiry date |
|---|---|
| F020 12002 | August 2016 |
Brief description of the problem
Recall because routine stability testing has indicated that this batch may go out of specification for potency before it expires.
Following a recently approved shelf-life extension, batch F020 12002 has a four year shelf-life. We understand that batches of this product released subsequently have had the original 3 year shelf-life reinstated.
Company contact for all enquiries
Syner-Medica Limited
Telephone: 0208 655 6393
Fax: 0208 655 6398
Email: sales@syner-med.com
Updated 22 December 2015. This page summarises an official notice. Details can change – always follow the official notice.